ClearanceBrief
510(k) K160806 ยท ITX Transducer, Ultrasonic, Diagnostic

Verza Guidance System

ApplicantCIVCO Medical Instruments Co., Inc., Kalona IA, US
DecisionSubstantially Equivalent, Aug 5, 2016
ReceivedMar 24, 2016
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K160806

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.